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SKP2 在癌症耐药性中的新兴作用。

Emerging Roles of SKP2 in Cancer Drug Resistance.

机构信息

Institute of Toxicology, School of Public Health, Lanzhou University, Lanzhou 730000, China.

Department of Pharmacology, College of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.

出版信息

Cells. 2021 May 10;10(5):1147. doi: 10.3390/cells10051147.

Abstract

More than half of all cancer patients receive chemotherapy, however, some of them easily acquire drug resistance. Resistance to chemotherapy has become a massive obstacle to achieve high rates of pathological complete response during cancer therapy. S-phase kinase-associated protein 2 (Skp2), as an E3 ligase, was found to be highly correlated with drug resistance and poor prognosis. In this review, we summarize the mechanisms that Skp2 confers to drug resistance, including the Akt-Skp2 feedback loop, Skp2-p27 pathway, cell cycle and mitosis regulation, EMT (epithelial-mesenchymal transition) property, enhanced DNA damage response and repair, etc. We also addressed novel molecules that either inhibit Skp2 expression or target Skp2-centered interactions, which might have vast potential for application in clinics and benefit cancer patients in the future.

摘要

超过一半的癌症患者接受化疗,但其中一些人很容易产生耐药性。化疗耐药性已成为癌症治疗中实现高病理完全缓解率的巨大障碍。S 期激酶相关蛋白 2(Skp2)作为一种 E3 连接酶,与耐药性和预后不良高度相关。在这篇综述中,我们总结了 Skp2 赋予耐药性的机制,包括 Akt-Skp2 反馈环、Skp2-p27 途径、细胞周期和有丝分裂调节、EMT(上皮-间充质转化)特性、增强的 DNA 损伤反应和修复等。我们还讨论了抑制 Skp2 表达或靶向以 Skp2 为中心相互作用的新型分子,这些分子在临床上可能具有巨大的应用潜力,并将有益于未来的癌症患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fe0/8150781/7b672271f85e/cells-10-01147-g001.jpg

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